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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474321Generated: October 29, 2026

Cyclohexylamine → 5-chloro-N-cyclohexylpyrazolo[1,5-c]pyrimidine-3-carboxamide

https://huagongshe.com/reaction/474321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
Reactant5-Chloropyrazolo[1,5-c]pyrimidine-3-carbonyl chlorideHCID 86661439—
SolventDichloromethaneHCID 6344—
Product5-chloro-N-cyclohexylpyrazolo[1,5-c]pyrimidine-3-carboxamideHCID 86661438100%

Reaction Steps

To a stirred solution of crude 5-chloropyrazolo[1,5-c]pyrimidine-3-carbonyl chloride (200 mg, 0.9 mM, 1.0 equiv) in 15 mL of dichloromethane was added cyclohexylamine (400 ul, 4.0 mM, 4 equiv). The reaction mixture was stirred for 15 minutes then quenched with 0.4 mL of acetic acid. The reaction mixture was concentrated under reduced pressure and the residue partitioned between water and dichloromethane. The dichloromethane phase was concentrated, and the crude product purified by flash chromatography on silica gel (97:3 dichloromethane:methanol) to yield 310 mg (100%) of 5-chloro-N-cyclohexylpyrazolo[1,5-c]pyrimidine-3-carboxamide. LCMS (ESI) m+H=279.1; 1H NMR (400 MHz, CDCl3) δ: 8.66 (s, 1H), 8.65 (d, 1H), 7.47 (d (broad exchangeable) 1H), 6.93 (d, 1H), 4.08 (m, 1H), 2.02 (m, 2H), 1.80 (m, 2H), 1.62 (m, 1H), 1.40 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637526B2
Source datasetuspto-grants-2014_01
ORD IDord-79952759a8004510b6356f8438a3c7b6
Source noteuspto-grants-2014_01